Dementia and Geriatric Cognitive Disorders · 2010 · 39 citations · 15 references
MedicineNeurologyNeuroscienceDementiaMolecular NeuroscienceNeurodegenerationAlzheimer DiseaseCerebrospinal Fluid BiomarkersDementia BiomarkersFrontotemporal DementiaNeurodegenerative DiseasesNeurodegenerative DisordersAlzheimer Disease DementiaAlzheimer Disease Tau PathologyAmyloid Beta PeptidesAmyloid Beta PlaquesCerebrospinal Fluid Neurodegeneration MarkersCerebrospinal Fluid SystemCerebrospinal Fluid TauTau Protein Biomarkers
BACKGROUND: Recent genetic and pathological studies have suggested that a lipoprotein receptor, LR11, is intricately implicated in the pathogenesis of Alzheimer disease (AD). We have recently established a novel sandwich ELISA, which enabled the sensitive quantification of a soluble LR11 (sLR11). By this ELISA, we attempted to determine the difference in the levels of CSF sLR11 in AD patients. METHODS: We examined CSF from 29 AD patients, 20 frontotemporal lobar degeneration patients and 27 age-matched control subjects. The CSF sLR11 level as well as the levels of tau and beta-amyloid42 (Abeta42) were determined by sandwich ELISA. RESULTS: The CSF tau level and tau/Abeta42 ratio were significantly increased (p < 0.01) in the AD patients. The CSF sLR11 level in the AD patients was significantly higher (p < 0.01) than that of the frontotemporal lobar degeneration patients and the controls. The APOE-epsilon4-positive AD patients have higher sLR11 levels than the APOE-epsilon4-negative patients (p < 0.01). CONCLUSIONS: These results suggest that the quantification of CSF sLR11 may serve as a biomarker of AD, although the diagnostic value for individual patients is limited. An elevated CSF sLR11 level in AD patients may be relevant to AD pathogenesis.
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